반응 #80662

ord-21f1a0c659a54c2aa7f296650f587aa8

반응 방정식

[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
Cc1ccc2c(c1)OC(C)(C)CC2(C)C
2,2,4,4,7-pentamethyl-chroman
Cc1ccc2c(c1)OC(C)(C)CC2(C)C
Compound 46
Cc1ccc2c(c1)OC(C)(C)CC2(C)C
2,2,4,4,7-pentamethyl-chroman
Cl
HCl
CC(=O)Cl
acetyl chloride
CC(=O)c1cc2c(cc1C)OC(C)(C)CC2(C)C
title compound
CC(=O)c1cc2c(cc1C)OC(C)(C)CC2(C)C
2,2,4,4,7-Pentamethyl-6-acetyl-chroman

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled in an ice-bath
  2. 2
    기타was waned to room temperature
  3. 3
    기타The organic layer was separated
  4. 4
    추출the aqueous layer extracted with ether
  5. 5
    세척washed successively with water, saturated NaHCO3 solution, water again
  6. 6
    건조saturated NaCl solution, and then dried (MgSO4)
  7. 7
    기타The solvent was removed in vacuo
  8. 8
    기타the residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes)

실험 절차

To an ice-bath cooled solution of 1.96 g (9.6 mmol) of 2,2,4,4,7-pentamethyl-chroman (Compound 46) in 30 ml of nitromethane was added under argon 1.059 g (13.5 mmol) of acetyl chloride followed by 1.9 g (14.3 mmol) of aluminum chloride. The reaction mixture was stirred at room temperature for 14 h and then cooled in an ice-bath and treated with 25 ml of conc. HCl. The mixture was waned to room temperature and diluted with ether and water. The organic layer was separated and the aqueous layer extracted with ether. The organic extracts were combined and washed successively with water, saturated NaHCO3 solution, water again, and saturated NaCl solution, and then dried (MgSO4). The solvent was removed in vacuo and the residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as a pale yellow oil. PMR (CDCl3): & 1.36 (6H, s), 1.37 (6H, s), 1.86 (2H, s), 2.49 (3H, s), 2.56 (3H, s), 6.65 (1H, s), 7.74 (1H, s).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05616597uspto-grants-1997_04